A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950263



Internal ID22725669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46769512..46773216hg38UCSC Ensembl
chr20:45398151..45401855hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg383705
hg193705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950263
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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